Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations-Reference-Cited by-同舟云学术

Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations

Published:2019-02 Issue: Volume:489 Page:103-108
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Fu Chunyun^ORCID,Luo Shiyu,Zhang Yue,Fan Xin,D'Gama Alissa M.,Zhang Xiaofei,Zheng Haiyang,Su Jiasun,Li Chuan,Luo Jingsi,Agrawal Pankaj B.,Li Qifei,Chen Shaoke

Funder

Guangxi Natural Science Foundation Program

Project of Yu-Miao

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference33 articles.

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3. The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH;Fu;Endocrin. Connect.,2017

4. Expanding the clinical spectrum associated with GLIS3 mutations;Dimitri;J. Clin. Endocrinol. Metab.,2015

5. A hot-spot mutation in CDC42 (p. Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome;Motokawa;J. Hum. Genet.,2018

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